Facility
MAQ-OPS, S. DE R.L.
1 recall(s) on record — most severe on record: Class III.
| FDA Establishment Identifier (FEI) | 3017550662 |
|---|---|
| Establishment type | Manufacture Medical Device |
| Location | Calle Guerrero Negro 9942 Tijuana Baja California, MX 22644 |
| Registration status | Active · expires 2026 |
| Parent company | ACON Laboratories, Inc. (owner-operator 9063887) |
Devices registered here (1)
- Covid-19 Multi-Analyte Antigen DeviceProduct code QMN · Not classified · Unknown
Recalls & enforcement
- Class IIITerminated2015-06-17Acon Laboratories, Inc. is recalling Mission Breath Alcohol Detector due to a labeling amendment.
Related
Source: U.S. FDA via openFDA (device registration & enforcement). Data as of 2026-08-13. Verify this facility record at FDA →
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